Slassi A - Search Results

1

3-(2-pyrrolidin-1-ylethyl)-5-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole derivatives as high affinity human 5-HT(1B/1D) ligands.

Egle I, MacLean N, Demchyshyn L, Edwards L, Slassi A, Tehim A. Egle I, et al. Among authors: slassi a. Bioorg Med Chem Lett. 2004 Feb 9;14(3):727-9. doi: 10.1016/j.bmcl.2003.11.023. Bioorg Med Chem Lett. 2004. PMID: 14741277

2

1-(Bicyclopiperazinyl)ethylindoles and 1-(homopiperazinyl)ethyl-indoles as highly selective and potent 5-HT(7) receptor ligands.

Isaac MB, Xin T, O'Brien A, St-Martin D, Naismith A, MacLean N, Wilson J, Demchyshyn L, Tehim A, Slassi A. Isaac MB, et al. Among authors: slassi a. Bioorg Med Chem Lett. 2002 Sep 2;12(17):2451-4. doi: 10.1016/s0960-894x(02)00438-9. Bioorg Med Chem Lett. 2002. PMID: 12161155

3

(R)-3-(N-methylpyrrolidin-2-ylmethyl)-5-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole derivatives as high affinity h5-HT1B/1D ligands.

Egle I, MacLean N, Demchyshyn L, Edwards L, Slassi A, Tehim A. Egle I, et al. Among authors: slassi a. Bioorg Med Chem Lett. 2003 Oct 20;13(20):3419-21. doi: 10.1016/s0960-894x(03)00779-0. Bioorg Med Chem Lett. 2003. PMID: 14505640

4

Pyrrolo[3,2,1-ij]quinoline derivatives, a 5-HT2c receptor agonist with selectivity over the 5-HT2a receptor: potential therapeutic applications for epilepsy and obesity.

Isaac M, Slassi A, O'Brien A, Edwards L, MacLean N, Bueschkens D, Lee DK, McCallum K, De Lannoy I, Demchyshyn L, Kamboj R. Isaac M, et al. Among authors: slassi a. Bioorg Med Chem Lett. 2000 May 1;10(9):919-21. doi: 10.1016/s0960-894x(00)00141-4. Bioorg Med Chem Lett. 2000. PMID: 10853660

5

5-Alkyltryptamine derivatives as highly selective and potent 5-HT1D receptor agonists.

Slassi A, Edwards L, O'Brien A, Meng CQ, Xin T, Seto C, Lee DK, MacLean N, Hynd D, Chen C, Wang H, Kamboj R, Rakhit S. Slassi A, et al. Bioorg Med Chem Lett. 2000 Aug 7;10(15):1707-9. doi: 10.1016/s0960-894x(00)00322-x. Bioorg Med Chem Lett. 2000. PMID: 10937729

6

6-Bicyclopiperazinyl-1-arylsulfonylindoles and 6-bicyclopiperidinyl-1-arylsulfonylindoles derivatives as novel, potent, and selective 5-HT6 receptor antagonists.

Isaac M, Slassi A, Xin T, MacLean N, Wilson J, McCallum K, Wang H, Demchyshyn L. Isaac M, et al. Among authors: slassi a. Bioorg Med Chem Lett. 2000 Aug 7;10(15):1719-21. doi: 10.1016/s0960-894x(00)00320-6. Bioorg Med Chem Lett. 2000. PMID: 10937732

7

Imidazoline-modified benzylimidazolines as h5-HT(1D/1B) serotonergic ligands.

Prisinzano T, Law H, Dukat M, Slassi A, MaClean N, Demchyshyn L, Glennon RA. Prisinzano T, et al. Among authors: slassi a. Bioorg Med Chem. 2001 Mar;9(3):613-9. doi: 10.1016/s0968-0896(00)00275-3. Bioorg Med Chem. 2001. PMID: 11310595

8

2-(Anilino)imidazolines and 2-(benzyl)imidazoline derivatives as h5-HT1D serotonin receptor ligands.

Prisinzano T, Dukat M, Law H, Slassi A, MacLean N, DeLannoy I, Glennon RA. Prisinzano T, et al. Among authors: slassi a. Bioorg Med Chem Lett. 2004 Sep 20;14(18):4697-9. doi: 10.1016/j.bmcl.2004.06.085. Bioorg Med Chem Lett. 2004. PMID: 15324890

9

N1-(Benzenesulfonyl)tryptamines as novel 5-HT6 antagonists.

Tsai Y, Dukat M, Slassi A, MacLean N, Demchyshyn L, Savage JE, Roth BL, Hufesein S, Lee M, Glennon RA. Tsai Y, et al. Among authors: slassi a. Bioorg Med Chem Lett. 2000 Oct 16;10(20):2295-9. doi: 10.1016/s0960-894x(00)00453-4. Bioorg Med Chem Lett. 2000. PMID: 11055342

10

5,5-Diaryl-2-amino-4-pentenoates as novel, potent, and selective glycine transporter type-2 reuptake inhibitors.

Isaac M, Slassi A, Silva KD, Arora J, MacLean N, Hung B, McCallum K. Isaac M, et al. Among authors: slassi a. Bioorg Med Chem Lett. 2001 Jun 4;11(11):1371-3. doi: 10.1016/s0960-894x(01)00253-0. Bioorg Med Chem Lett. 2001. PMID: 11378357

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